Device recall
Z-2135-2014: Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc Syringe…
FDA device recall · Class I · Enhancement Medical, LLC
Key facts
| Recall number (Z-number) | Z-2135-2014 |
|---|---|
| Recall event | 68596 |
| Product | Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc Syringe with hyaluronic acid concentration of 20 mg/ml. Product Usage: Expression is labelled as an Intranasal Splint, intended to minimize bleeding and edema and to prevent adhesions between the septum and the nasal cavity… |
| Product code | LMH |
| Recalling firm | Enhancement Medical, LLC |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 29, 2017 |
| FEI number | 3008404291 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database